Keywords
Climate change, Translocation, Conservation Biology, Ecological Restoration, Terrestrial Ecosystems, Species Interactions
Climate change, Translocation, Conservation Biology, Ecological Restoration, Terrestrial Ecosystems, Species Interactions
Populations of animals and plants facing insurmountable barriers to dispersal, and species with low dispersal abilities are likely to be highly impacted by climate change1. With temperatures changing in their historical distribution area, such species may not be able to colonise new habitats with more hospitable climatic conditions and may require human intervention in the form of assisted colonisation if they are to survive2,3.
The translocation of endangered species has been used as a conservation management tool for several decades4,5 and assisted colonisation as defined by Ricciardi & Simberloff (2009) appears as a logical tool for mitigating the impact of climate change on terrestrial organisms7. However, conservation translocations can be logistically difficult and costly8 and can often fail7,9,10. One potential cause of failure is that the complex community interactions of which the translocated species are a part are left behind. Such interactions are likely to be required for long-term survival of the target species but may not be present or fully functioning at the appropriate rate at the translocation site11. These interactions are also likely to be the first component of the ecosystem to be impacted by climate change12, long before any population or species goes extinct. Conservation strategies should therefore have a greater focus on the translocation of whole ecosystems and their inherent interactions rather than that of individual ‘flagship’ species13. This paper explores a novel approach – ecosystem-scale translocation (EST) – as a means to preserve functioning terrestrial ecosystems threatened by climate change. This involves the careful collection and immediate transfer of topsoil, vegetation and associated ecological communities to a receptor site. Ecosystem-scale translocation may represent an immediately available and practical method for preserving communities and ecosystems threatened by climate change. Here, with the aim of fostering discussion and debate about the EST concept, we 1) outline the possible promises and pitfalls of EST in mitigating the impact of climate change on terrestrial biodiversity and 2) use a GIS-based approach to illustrate how potential source and receptor sites, where EST could be trialed and evaluated globally, could be identified.
Species interactions are essential to the functioning of ecosystems. However, in the context of climate change and biodiversity crises, understanding the full range of community interactions that are needed to recreate a functioning ecosystem in a potential receptor area is not realistic14. It follows that ecological engineering through manual planting or regeneration through the seedbank, as is applied in classical restoration programmes15, is not a practical solution for conserving functioning above- and below-ground communities of ecosystems threatened by climate change. On the contrary, the translocation of topsoil, vegetation and all the communities they contain could represent a much-needed shortcut where all components and interactions of an ecosystem are potentially preserved.
Under the terms habitat translocation, community translocation, vegetation translocation or transplanting, ecosystem translocation has been applied at a small scale to conserve particular plant species or communities impacted by proposed land development16 but also to test the robustness of plant communities in climatically challenging conditions11,17. A number of earlier translocation attempts reviewed by Good et al.18 showed that with appropriate preparation of the receiver sites, translocation of turves produced satisfactory results in terms of plant survival and conservation of community composition for a variety of plant community types. In the mining industry, a similar process called vegetation direct transfer (VDT) has been applied for 30 years as part of mine restoration programmes19–21 sometimes translocating large areas. For example, a total of 75 ha of native grassland, shrubland and low canopy forest have been translocated within the Stockton Mine (New Zealand) in the past 30 years22–24. The method used consists of (i) cutting pieces of land comprising soil, roots and vegetation over a 1–3 m2 area and a depth of 30 cm or more using a digger, (ii) transporting these sods by truck to a new area and (iii) reconstituting the ‘jigsaw’ with minimum gaps between the sods to recreate a continuous habitat (Figure 1). Many studies have highlighted the positive outcomes of such translocations, including: the conservation of plant and beetle communities, soil functions and microbial activity after wetland translocation25,26; the maintenance of soil structure and fertility in translocated grassland; rtebrates (e.g. carabid beetles, weta) and plant species (beech) from shrubland and tussock wetlands22; the preservation of biodiversity and biomass in soil fauna27 and microbial communities28 from alpine vegetation; and the conservation of habitat for birds and invertebrates from translocated forest areas21. There is also an extensive body of work, including peer-reviewed articles21,24,26,29 and reviews18,19,21, but also internal reports and conference presentations (see Supplementary material), most of which point to the conclusion that VDT promotes faster ecosystem recovery than do other conventional restoration techniques such as replanting or hydroseeding.
Clockwise: pieces of land comprising vegetation, roots and soil are cut; soil and vegetation sods are loaded on a truck and transported to the receptor site; the landscape jigsaw is then reconstituted with minimum gaps between the sods to recreate a continuous habitat. Credits: Stéphane Boyer and Solid Energy New Zealand Ltd.
Could ecosystem-scale translocation represent a practical and economic translocation method, by which all or most immobile, slow moving and low-dispersal elements of a terrestrial ecosystem are moved together as a functioning community of above- and below-ground organisms? While no taxonomic group is particularly targeted by EST, it is likely that plant, microbial and fungal communities as well as most invertebrates and small vertebrates will directly benefit, while large and mobile terrestrial vertebrates will probably vacate the site due to disturbance during the translocation process. Therefore, EST constitutes a complementary approach to single-species conservation translocation programs, which suffer from a significant taxonomic bias towards larger animals. Indeed, almost 60% of all animal translocation efforts to date have been for large and charismatic species of birds and mammals7, despite these taxa comprising only c. 1% of all known animal species30. Although translocation distances and the sizes of the areas translocated are usually minimised for economic and practical reasons in a restoration context (Figure 2), this process could be scaled up for the purpose of ESTs where the aim is to mitigate the impact of climate change on biodiversity in highly-valued ecosystems. The aim of EST should be to preserve a functioning representative subset of an ecosystem of sufficient size to ensure its long-term survival and functioning. Capturing most ecosystem functions is likely to require the translocation, in stages, of fairly large areas. However, the majority of the current protected areas globally are less than 1,000 ha and places such as Barro Colorado in Panama (1,500 ha), the Bosavi Crater in Papua New Guinea (1,250 ha), or Darwin Island in the Galapagos (110 ha), are good examples of relatively small areas with significant biodiversity interest.
The orange area corresponds to typical past and current habitat translocation projects, with dots corresponding to published studies (see Supplementary material S1 for a complete list). The green area represents an ideal combination of size and distance for ecosystem-scale translocation, with darker green more suitable, although more difficult to put in place.
Only a handful of translocation studies have been reported in the scientific literature (Supplementary material) and the extent to which biodiversity conservation was measured in these studies is very limited. More targeted research is therefore required to assess to what extent EST can conserve biodiversity at a range of levels including species, genetic and functional diversity, as well as species interactions and ecosystem functions. Critical factors and recommendations required for habitat translocation include similarity between the environmental conditions of the donor and receptor sites, the translocation technique, and appropriate management of the translocated habitat31. In particular, the nature of the bedrock strata as well as the geochemistry, hydrology and precipitations at the receptor site will have a strong influence on the translocated topsoil. Geology can be measured and matched between donor and receptor sites, while the range of possible changes in fine-scale hydro-dynamics may be much more difficult to predict as climate changes32. One additional and outstanding issue is the selection of a candidate receptor site where the ‘graft’ will not replace communities which are themselves of high-value, possibly leading to the extinction of local species14 or negatively impacting the functioning of surrounding ecosystems6,9. For example, some phytophagous insects could rapidly become invasive when encountering new plant species within their distribution range33. Conversely, the spillover of existing invasive species from areas surrounding the receptor site could negatively impact the graft itself. This is possibly of less concern because species invasion is less likely to happen when translocating complete and functioning ecosystems where most or all niches are occupied and, consequently, where the lack of empty niches make ecosystems more resistant to the establishment of invasive species34. Supposedly, invasion risk could also be reduced if the receptor site is located, within areas where species composition does not differ dramatically from that of the donor site. Nevertheless, it is important to note that any negative impacts are likely to be difficult and costly to reverse after translocation and a thorough risk assessment would be required to ensure that translocated species do not affect the surrounding areas after translocation.
The cost involved in the translocation of ecosystems is likely to constitute an important limitation. Because only few examples exist, it is difficult to provide a definite price per unit area. One comparative study by Simcock et al.22 showed that translocation in a mine rehabilitation context was seven times more costly than transporting bulldozed soil and vegetation, but twice cheaper than rehabilitation through nursery cultivation followed by manual replanting. This study was based on the translocation of a 0.6 ha of native forest over a few hundred meters distance and most of the additional cost was from transportation between donor and receptor area as trucks could only carry a single layer of sods (i.e. 30 to 50% of full capacity)22. Translocation of larger areas over much longer distances, as required for EST (Figure 2), is likely to be much more costly.
In addition to a deep understanding of the risks and potential side effects, the application of EST also requires carefully selected receptor sites. Suitable receptor sites should have very low intrinsic biodiversity value because they will be replaced by EST and whatever communities were present will disappear. Such potential sites could be selected in agricultural land that has been marginalised or abandoned due to the erosion of the fertile soil layer and the loss of essential soil nutrients following overexploitation or misuse35. It has recently been estimated that 25% of all terrestrial habitat is highly degraded36, with one hectare of productive land lost globally every 7.67 seconds (www.irri.org). There is growing interest in using such marginal and degraded land to cultivate biofuel crops37,38. However, this land could alternatively be used for biological conservation. When soil is lost or degraded to the extent where growing crops is not possible, the land could still be suitable for receiving EST, because the latter includes topsoil and its associated ecosystem functions. With human-degraded soils scattered across all continents37 potential receptor sites could be available in a range of climate zones.
Assisted colonisation of single species includes moving organisms to habitats with more favorable future climatic conditions5. The timing of assisted colonisation is therefore crucial because those performed before the recipient region is predicted to be climatically suitable are likely to fail39. Determining the “window of opportunity” – a scenario where an ecosystem is still viable at its original location, and where there is an existing suitable receptor site - is likely to prove difficult and will require active adaptive management40. To alleviate the above limitation, EST could be applied to move ecosystems from climatically unstable areas to areas where the climate is projected to remain stable despite global changes41. The climate stability index proposed by Iwamura et al.42 can be used in this context. This index compares observed temperature, precipitation, cloud cover and vapour pressure in 1997–2002 to projected values in 2047–2052. Human-degraded soils that occur in climatically stable areas could offer prime locations to receive ESTs and could receive them from regions of high conservation value (e.g. biodiversity hotspots) currently located in unstable climatic areas.
Using a highly conservative GIS approach (see Method section), we identified a range of potential source and receptor areas at a global scale. The former were located mainly in North America and North Eurasia as well as over the Amazonian forest (Figure 3A), while a large majority of potential receptor areas were located in Africa, with smaller areas also identified in America, the Middle East, Asia and Australasia (Figure 3B). The suitability of these source and receptor areas is largely dependent on the accuracy of current climatic predictive models, which are constantly improving43. Also, climatic stability thresholds and criteria used for selecting highly valuable ecosystems or degraded land can vary greatly. In a similar way to conservation programmes, which often struggle to cross borders44 due to different policy in neighbouring countries and a lack of global legislation, EST is highly unlikely to be applied in a cross-border situation (where an ecosystem with high conservation value would be translocated from one country to another). Therefore, we identified countries where large areas of both source and receptor sites were present (Figure 3C). They include Madagascar, USA (California), Mexico, Turkey, Nigeria, Cameroon, South Africa, Vietnam, Thailand, Myanmar and Indonesia (Table 1). These countries may therefore be ideal candidates to trial EST.
Ideal source areas are those where high value (blue lines) overlaps with low climatic stability (in pink).
Ideal sites are those where high soil degradation (red lines) overlaps with high climatic stability (in purple).
Countries were ranked from best to worst candidates based on size of source area, size of receptor area and minimum distance between the two. Orange background: best candidate countries based on thresholds of 15,000 km2 for the areas and 500 km distance between areas. Numbers in bold correspond to limiting factors. Blue background: countries where distance between source and receptor may be limiting using the above criteria; Purple background: countries where receptor areas may be limiting; Green background: countries where receptor areas may be limiting; Grey background: countries where multiple limiting factors exist. Min. source-receptor distance is the minimum distance between a patch of source area and a patch of receptor area. When source and receptor are adjacent, the minimum source-receptor distance is 0.
Clear evidence that ecosystems have started to shift in response to climate change is now observable, with plant45 and animal46 advancing towards higher altitudes and latitudes. Using the EST approach, it may be possible to move ecosystems as a preemptive measure to ensure that all immobile, slow moving and low-dispersal elements of a terrestrial ecosystem are moved together as a functioning community of above- and below-ground organisms.
Translocating communities and ecosystems should not be regarded as a substitute for less invasive conservation efforts when such options are available19,47, but considered only as a last resort, when ecosystems are at inevitable risk of disappearance or collapse. In the review by Bullock (1998), community translocation often did not achieve the preservation of complete and unchanged community, but led to communities ‘which resembles the pre-translocated state in mitigation for the loss of the original community and which retains many of the species found at the donor site. This method should therefore be recommended only when the aim is to mitigate inevitable negative impact on high-valued ecosystems. Important considerations associated with the proposed approach include the differences in bedrock strata, geochemistry and hydro-dynamics between the source and receptor site, the size of the translocated ecosystem subset in relation to edge effects and isolation, and potential negative impacts on the receptor site. These limitations will require careful planning on a case-by-case basis to minimise the risks of failure. However, in the face of the urgency of climate change, there is a pressing need for proposing and testing more proactive and ambitious forms of conservation management. Hoping that most species threatened by climate change will be able to (i) use environmental buffering48; (ii) retreat to refugia49; (iii) follow their climatic niche, potentially with the help of ‘corridors’50; or (iv) exhibit some form of phenotypic plasticity or micro-evolution on very short time-scales51 is unlikely to be sufficient to conserve biodiversity at all scales. Ecosystem-scale translocation adds to the current debate on novel and audacious ideas to stem biodiversity loss, which include de-extinction52 and the setting aside of half the planet for wildlife as proposed by E.O Wilson53. Our analysis provides a starting point for discussion about the potential of EST for the conservation of ecosystems threatened by climate change. Although this is undoubtedly a radical option, and one that should be examined with caution, it could be applied to conserve very highly-valued ecosystems. Even if a number of species or functions were to be lost during the translocation process, this approach would still improve on the current limited single-species conservation translocation strategies. The EST approach is particularly suited to the conservation of small life forms, thereby balancing the current bias toward translocation and conservation of birds and mammals7 and addressing the urgent issue of conserving invaluable invertebrate communities54. This approach has the potential to add a new dimension to the spectrum of conservation tools currently available, with the aim of conserving mature and complex terrestrial ecosystems threatened by climate change.
Research is urgently required to assess to what extent EST can conserve not only species diversity, but also genetic diversity, functional diversity, species interactions and ecosystem functions. Source and receptor sites that ranked highly in this study would provide ideal candidates to test these hypotheses in medium to large-scale experiments of EST. This information will be critical to inform future EST projects, which are likely to become necessary if we are to tackle one of the biggest ecological challenges of the coming decades: preserving biodiversity at the ecosystem scale in an era of unprecedented climate change.
Literature included in Figure 2 was selected using the keywords ‘vegetation direct transfer’, ‘habitat translocation’, ‘vegetation translocation’, ‘community translocation’ and ‘vegetation transplant’ in all databases available in ISI Web of Science. This search was restricted to English written articles published from 1910 to 2016 (search conducted in January 2016). The reference lists of papers retrieved using these searches were then screened based on their titles for potential additional references. We used only those articles where the size of area translocated was reported and translocation distance was either given or could be estimated based on maps or GPS coordinates. Additional publications were extracted from the database of Solid Energy New Zealand Ltd. (www.solidenergy.co.nz) and Landcare Research (http://www.landcareresearch.co.nz) using the same search terms. All information used to build Figure 2 is summarised with the corresponding references in the Supplementary material.
We mapped the location of potential areas where EST may be applicable on a global scale by overlaying the GIS maps described below using ArcGIS 10.1. Potential source areas for EST were identified in GIS as those predicted to have a relatively unstable future climate based on global climate models, while also having high global conservation value. Climatically-unstable areas were identified using an ecoregion-based climate stability index dataset41,55, which incorporates seven different future climatic scenarios, and indicates how different future climate will be compared to present climate. This index ranges from 0.0 to 1.0 where 1.0 corresponds to complete overlap between current and future climates while 0.0 indicates no overlap55. We averaged the climate stability indices across these seven climate scenarios; relatively climatically-unstable ecoregions were identified as those that had a mean stability index of <0.33 (Figure 3A – pink areas). Areas of high global conservation values were identified using the Conservation International Biodiversity Hotspots dataset56 (Figure 3A – blue outlined areas). Potential receptor sites for EST were delineated in the GIS as areas that have both relatively high predicted future climate stability and a high incidence of soil degradation. Climatically stable areas were identified as ecoregions with a mean stability index of >0.66 (Figure 3B – purple areas). Highly-degraded areas (Figure 3B – red outlined areas) were extracted from a global soil degradation GIS dataset (GLASOD57) as those polygons comprising degradation categories 3 and 4. The final composite map (Figure 3C) shows the position of potential source and receptor sites together overlaid with country boundaries. For each country containing both source and receptor sites, we then calculated the total area of, and minimum distances between source and receptor sites within each country, allowing us to rank their potential as candidates for EST (Table 1). We considered countries with source and receptor areas greater than 15,000 km2 as good candidates because they offer a greater range in the choice of possible source and receptor sites. The other characteristic taken into account was the minimum distance between source and receptor areas. When this distance was less than 500 km, countries were ranked highly because road transportation is more likely to be completed within one day, therefore minimising the impact on the integrity of the transported vegetation and soil.
S.B. developed the concept and designed the manuscript. B.S.C. ran the GIS analysis and produced the maps. S.B. and B.S.C. prepared the figures and tables. S.B., B.S.C, M.-C.L., B.R.W. and S.D.W wrote the manuscript.
We are grateful to Solid Energy New Zealand Ltd. and Bathurst Resources Limited for providing information about their restoration programmes as well as internal reports.
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Competing Interests: No competing interests were disclosed.
Competing Interests: No competing interests were disclosed.
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